Variant #0010001422 (NC_000016.9:g.70323619G>T, NM_001605.2:c.-317C>A (AARS))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.70323619G>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/123150
gnomAD homozygote count 0/61572
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
DDX19B NM_001257174.1 ./. c.-460G>T r.(=) p.(=)
AARS NM_001605.2 ./. c.-317C>A r.(=) p.(=)